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Zangerl, Barbara

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Bestrophin gene mutations cause canine multifocal retinopathy : a novel animal model for best disease 17 15 0
Modeling the structural consequences of BEST1 missense mutations 17 16 0
Independent origin and restricted distribution of RPGR deletions causing XLPRA 10 10 0
Identification of genetic variation and haplotype structure of the canine ABCA4 gene for retinal disease association studies 44 39 0
Assessment of canine BEST1 variations identifies new mutations and establishes an independent bestrophinopathy model (cmr3) 11 9 0
Molecular consequences of BEST1 gene mutations in canine multifocal retinopathy predict functional implications for human bestrophinopathies 11 11 0
RPGRIP1 and cone-rod dystrophy in dogs 36 32 2
Canine multifocal retinopathy in the Australian Shepherd : a case report 27 25 0
Structural organization and expression pattern of the canine RPGRIP1 isoforms in retinal tissue 10 10 0
Comparative genomic mapping of uncharacterized canine retinal ESTs to identify novel candidate genes for hereditary retinal disorders 18 18 0
Familial cutaneous lupus erythematosus (CLE) in the German shorthaired pointer maps to CFA18, a canine orthologue to human CLE 57 49 0
Transcriptional profile analysis of RPGRORF15 frameshift mutation identifies novel genes associated with retinal degeneration 20 19 0
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Zangerl, Barbara

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Zangerl, Barbara

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